Canonical Allele Identifier: CA1140726319

Gene: FMO3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171114092G= , CM000663.2:g.171114092G=	GRCh38
NC_000001.10:g.171083232G= , CM000663.1:g.171083232G=	GRCh37
NC_000001.9:g.169349856G=	NCBI36
NG_012690.1:g.28215G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367755.9:c.913G= MANE Select	ENSP00000356729.4:p.Glu305=
ENST00000367755.8:c.913G=	ENSP00000356729.4:p.Glu305=
NM_001002294.2:c.913G=	NP_001002294.1:p.Glu305=
NM_006894.5:c.913G=	NP_008825.4:p.Glu305=
XM_005245044.1:c.724G=	XP_005245101.1:p.Glu242=
XM_011509345.1:c.853G=	XP_011507647.1:p.Glu285=
XM_011509346.1:c.853G=	XP_011507648.1:p.Glu285=
NM_001319173.1:c.853G=	NP_001306102.1:p.Glu285=
NM_001319174.1:c.724G=	NP_001306103.1:p.Glu242=
XM_011509345.3:c.853G=	XP_011507647.1:p.Glu285=
XM_024454365.1:c.166G=	XP_024310133.1:p.Glu56=
NM_001002294.3:c.913G= MANE Select	NP_001002294.1:p.Glu305=
NM_001319173.2:c.853G=	NP_001306102.1:p.Glu285=
NM_001319174.2:c.724G=	NP_001306103.1:p.Glu242=
NM_006894.6:c.913G=	NP_008825.4:p.Glu305=